EP 0983390 A1 20000308 - INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE
Title (en)
INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE
Title (de)
DIAGNOSTISCHES VERFAHREN ZUR GENOTYPISIERUNG FAMILIÄRER HEMIPLEGISCHER MIGRÄNE VOM TYP 2
Title (fr)
METHODE DE DIAGNOSTIC GENOTYPIQUE INDIRECT DE LA MIGRAINE HEMIPLEGIQUE FAMILIALE DE TYPE 2
Publication
Application
Priority
- FR 9801162 W 19980608
- FR 9707033 A 19970606
Abstract (en)
[origin: FR2764306A1] The invention concerns an indirect genotypic method for diagnosing type 2 familial hemiplegic migraine in a person, characterised in that it consists in: isolating in said person's DNA the presence of a marker located on the 1a21-q23 chromosome in the locus limited by the D1S2343 and D1S2844 markers, said marker being related with the occurrence of familial hemiplegic migraine in his family.
IPC 1-7
IPC 8 full level
C12N 15/12 (2006.01); C12Q 1/68 (2006.01); C12Q 1/6883 (2018.01)
CPC (source: EP)
C12Q 1/6883 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/172 (2013.01)
Citation (search report)
See references of WO 9855647A1
Designated contracting state (EPC)
AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE
DOCDB simple family (publication)
FR 2764306 A1 19981211; FR 2764306 B1 20010810; CA 2292795 A1 19981210; EP 0983390 A1 20000308; WO 9855647 A1 19981210
DOCDB simple family (application)
FR 9707033 A 19970606; CA 2292795 A 19980608; EP 98929511 A 19980608; FR 9801162 W 19980608